CA2181129A1 - Revetements de silicone reticulables renfermant des siloxanes avec des groupes alcoxy et alcenyle - Google Patents

Revetements de silicone reticulables renfermant des siloxanes avec des groupes alcoxy et alcenyle

Info

Publication number: CA2181129A1
Authority: CA; Canada
Prior art keywords: group; value; me2sio; compound; r2sio
Prior art date: 1995-07-28
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

CA002181129A

Other languages

English (en)

Inventor

Michael Joseph Brasseur

Kun-Long Chen

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Silicones Corp

Original Assignee

Dow Corning Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-07-28

Filing date

1996-07-12

Publication date

1997-01-29

1996-07-12 Application filed by Dow Corning Corp filed Critical Dow Corning Corp

1997-01-29 Publication of CA2181129A1 publication Critical patent/CA2181129A1/fr

Status Abandoned legal-status Critical Current

Links

239000004447 silicone coating Substances 0.000 title claims abstract description 26
-1 siloxanes Chemical class 0.000 title claims description 70
125000003342 alkenyl group Chemical group 0.000 title abstract description 7
125000003545 alkoxy group Chemical group 0.000 title abstract description 4
239000000203 mixture Substances 0.000 claims description 82
150000001875 compounds Chemical class 0.000 claims description 69
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 65
238000000576 coating method Methods 0.000 claims description 32
239000011248 coating agent Substances 0.000 claims description 29
239000003054 catalyst Substances 0.000 claims description 28
239000003112 inhibitor Substances 0.000 claims description 23
239000004215 Carbon black (E152) Substances 0.000 claims description 19
229930195733 hydrocarbon Natural products 0.000 claims description 19
229910052751 metal Inorganic materials 0.000 claims description 19
239000002184 metal Substances 0.000 claims description 19
238000000034 method Methods 0.000 claims description 15
239000004606 Fillers/Extenders Substances 0.000 claims description 14
239000000758 substrate Substances 0.000 claims description 14
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 11
239000003085 diluting agent Substances 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 9
230000005855 radiation Effects 0.000 claims description 8
229920002554 vinyl polymer Polymers 0.000 claims description 8
239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 7
125000006043 5-hexenyl group Chemical group 0.000 claims description 6
239000008199 coating composition Substances 0.000 claims description 6
150000003961 organosilicon compounds Chemical class 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
150000002430 hydrocarbons Chemical class 0.000 claims description 5
150000001735 carboxylic acids Chemical class 0.000 claims description 4
229920001577 copolymer Polymers 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
150000004292 cyclic ethers Chemical class 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
125000000075 primary alcohol group Chemical group 0.000 claims description 2
125000003198 secondary alcohol group Chemical group 0.000 claims description 2
229920001296 polysiloxane Polymers 0.000 abstract description 17
239000000654 additive Substances 0.000 abstract description 10
230000000996 additive effect Effects 0.000 abstract description 4
229910052697 platinum Inorganic materials 0.000 description 23
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 12
239000000853 adhesive Substances 0.000 description 12
230000001070 adhesive effect Effects 0.000 description 12
150000003254 radicals Chemical class 0.000 description 12
239000000463 material Substances 0.000 description 11
239000000123 paper Substances 0.000 description 10
238000006116 polymerization reaction Methods 0.000 description 9
125000006038 hexenyl group Chemical group 0.000 description 8
FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
239000004615 ingredient Substances 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
235000019445 benzyl alcohol Nutrition 0.000 description 4
239000004927 clay Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
229920001843 polymethylhydrosiloxane Polymers 0.000 description 4
239000007787 solid Substances 0.000 description 4
ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 3
239000011888 foil Substances 0.000 description 3
230000005012 migration Effects 0.000 description 3
238000013508 migration Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920000098 polyolefin Polymers 0.000 description 3
230000003578 releasing effect Effects 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
235000008429 bread Nutrition 0.000 description 2
QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 2
150000005826 halohydrocarbons Chemical class 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
150000002688 maleic acid derivatives Chemical class 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920006267 polyester film Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
150000003333 secondary alcohols Chemical class 0.000 description 2
HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
150000004072 triols Chemical class 0.000 description 2
TXRSZYWHJFERCN-PLNGDYQASA-N (Z)-4-(1,2-dimethoxypropan-2-yloxy)-4-oxobut-2-enoic acid Chemical compound COCC(C)(OC)OC(=O)\C=C/C(O)=O TXRSZYWHJFERCN-PLNGDYQASA-N 0.000 description 1
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
YTTFFPATQICAQN-UHFFFAOYSA-N 2-methoxypropan-1-ol Chemical compound COC(C)CO YTTFFPATQICAQN-UHFFFAOYSA-N 0.000 description 1
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 1
JQZGUQIEPRIDMR-UHFFFAOYSA-N 3-methylbut-1-yn-1-ol Chemical compound CC(C)C#CO JQZGUQIEPRIDMR-UHFFFAOYSA-N 0.000 description 1
SJVGFKBLUYAEOK-SFHVURJKSA-N 6-[4-[(3S)-3-(3,5-difluorophenyl)-3,4-dihydropyrazole-2-carbonyl]piperidin-1-yl]pyrimidine-4-carbonitrile Chemical compound FC=1C=C(C=C(C=1)F)[C@@H]1CC=NN1C(=O)C1CCN(CC1)C1=CC(=NC=N1)C#N SJVGFKBLUYAEOK-SFHVURJKSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
SYKNUAWMBRIEKB-UHFFFAOYSA-N [Cl].[Br] Chemical compound [Cl].[Br] SYKNUAWMBRIEKB-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000002390 adhesive tape Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
GVTGUOINIMHIRT-WAYWQWQTSA-N bis(1-methoxypropan-2-yl) (z)-but-2-enedioate Chemical compound COCC(C)OC(=O)\C=C/C(=O)OC(C)COC GVTGUOINIMHIRT-WAYWQWQTSA-N 0.000 description 1
BGFNTZUTTUOBSW-FPLPWBNLSA-N bis(2-methoxypropan-2-yl) (z)-but-2-enedioate Chemical compound COC(C)(C)OC(=O)\C=C/C(=O)OC(C)(C)OC BGFNTZUTTUOBSW-FPLPWBNLSA-N 0.000 description 1
ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
239000008393 encapsulating agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000004744 fabric Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
150000004687 hexahydrates Chemical group 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052741 iridium Inorganic materials 0.000 description 1
GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical class CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
229960004592 isopropanol Drugs 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000002655 kraft paper Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000007769 metal material Substances 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920006136 organohydrogenpolysiloxane Polymers 0.000 description 1
229910052762 osmium Inorganic materials 0.000 description 1
SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
239000000565 sealant Substances 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/14—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane

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Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA002181129A 1995-07-28 1996-07-12 Revetements de silicone reticulables renfermant des siloxanes avec des groupes alcoxy et alcenyle Abandoned CA2181129A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US08/508,783		1995-07-28
US08/508,783 US5567764A (en)	1995-07-28	1995-07-28	Curable silicone coatings containing alkoxy and alkenyl functional siloxanes

Publications (1)

Publication Number	Publication Date
CA2181129A1 true CA2181129A1 (fr)	1997-01-29

Family

ID=24024055

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002181129A Abandoned CA2181129A1 (fr)	1995-07-28	1996-07-12	Revetements de silicone reticulables renfermant des siloxanes avec des groupes alcoxy et alcenyle

Country Status (7)

Country	Link
US (1)	US5567764A (fr)
EP (1)	EP0761790B1 (fr)
JP (1)	JPH09132755A (fr)
KR (1)	KR970006438A (fr)
CA (1)	CA2181129A1 (fr)
DE (1)	DE69600659T2 (fr)
TW (1)	TW336249B (fr)

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US6716533B2 (en)	2001-08-27	2004-04-06	General Electric Company	Paper release compositions having improved adhesion to paper and polymeric films
US7090923B2 (en)	2003-02-12	2006-08-15	General Electric Corporation	Paper release compositions having improved adhesion to paper and polymeric films
US7005475B2 (en) *	2003-06-10	2006-02-28	General Electric Company	Curable silicone compositions having improved adhesion to polymeric films
JP2005336270A (ja) *	2004-05-25	2005-12-08	Shin Etsu Chem Co Ltd	液状シリコーンゴムコーティング剤組成物およびエアーバッグ
WO2008005293A1 (fr) *	2006-07-07	2008-01-10	Henkel Corporation	Compositions de silicone rtv de faible module résistantes à l'humidité, et leurs procédés de préparation
US20110186790A1 (en) *	2009-07-23	2011-08-04	E. I. Du Pont De Nemours And Company	Fluorinated hybrid compositions
US20110189382A1 (en) *	2009-07-23	2011-08-04	E. I. Du Pont De Nemours And Company	Method of preparing fluorinated hybrid compositions
US20110200826A1 (en) *	2009-07-23	2011-08-18	E. I. Du Pont De Nemours And Company	Articles containing fluorinated hybrid compositions
WO2013022448A1 (fr)	2011-08-10	2013-02-14	Empire Technology Development Llc	Articles thermoplastiques dotés d'un revêtement détachable
KR101418012B1 (ko)	2012-06-08	2014-07-09	주식회사 케이씨씨	경화성 실리콘 조성물 및 이를 이용한 전자장치
KR101674630B1 (ko)	2015-05-08	2016-11-09	(주) 나눅스엔지니어링	헬멧 피팅 장치
US10093578B2 (en) *	2016-07-01	2018-10-09	Matthew Paul Elam	Asphalt crack filling system and method of use
KR101941119B1 (ko)	2017-04-17	2019-01-22	주식회사 디자인네오그룹	레저 스포츠용 헬멧
WO2020000387A1 (fr)	2018-06-29	2020-01-02	Dow Silicones Corporation	Additif d'ancrage et ses procédés de préparation et d'utilisation
US20210246337A1 (en)	2018-06-29	2021-08-12	Dow Silicones Corporation	Solventless silicone pressure sensitive adhesive and methods for making and using same
US10947386B2 (en)	2018-08-09	2021-03-16	Matthew Paul Elam	Method and system of anti-stripping process using organosilanes and lime to manufacture asphalt
JP2023530836A (ja) *	2020-06-22	2023-07-20	ダウシリコーンズコーポレーション	低強度放射線硬化性シリコーン剥離コーティング組成物並びにその調製及び使用のための方法
CN115975200B (zh) *	2022-12-27	2023-07-18	杭州崇耀科技发展有限公司	一种硅油离型剂用锚固剂及其使用方法

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1995
- 1995-07-28 US US08/508,783 patent/US5567764A/en not_active Expired - Fee Related
1996
- 1996-07-05 TW TW085108152A patent/TW336249B/zh active
- 1996-07-12 EP EP96111256A patent/EP0761790B1/fr not_active Expired - Lifetime
- 1996-07-12 CA CA002181129A patent/CA2181129A1/fr not_active Abandoned
- 1996-07-12 DE DE69600659T patent/DE69600659T2/de not_active Expired - Fee Related
- 1996-07-26 KR KR1019960030597A patent/KR970006438A/ko not_active Abandoned
- 1996-07-26 JP JP8197990A patent/JPH09132755A/ja not_active Withdrawn

Also Published As

Publication number	Publication date
JPH09132755A (ja)	1997-05-20
US5567764A (en)	1996-10-22
DE69600659D1 (de)	1998-10-22
EP0761790B1 (fr)	1998-09-16
EP0761790A1 (fr)	1997-03-12
KR970006438A (ko)	1997-02-21
TW336249B (en)	1998-07-11
DE69600659T2 (de)	1999-05-06

Legal Events

Date	Code	Title	Description
2011-02-01	FZDE	Discontinued	Effective date: 20020712

Publication	Publication Date	Title
CA2181129A1 (fr)	1997-01-29	Revetements de silicone reticulables renfermant des siloxanes avec des groupes alcoxy et alcenyle
US5036117A (en)	1991-07-30	Heat-curable silicone compositions having improved bath life
AU722491B2 (en)	2000-08-03	Silicone release coating compositions
CA1174394A (fr)	1984-09-11	Revetements antiaherents a base de silicone et inhibiteurs
EP0605227B1 (fr)	1998-11-18	Compositions pour augmenter la force de décollage de revêtements silicone papier anti-adhésifs
US4774111A (en)	1988-09-27	Heat-curable silicone compositions comprising fumarate cure-control additive and use thereof
US5708046A (en)	1998-01-13	Silicone release coating compostions
CA1234245A (fr)	1988-03-15	Procede de revetement et compositions d'organopolysiloxane reticulables par l'humidite utilisees a cette fin
US5696211A (en)	1997-12-09	Silicone release coating compositions
US5468828A (en)	1995-11-21	Silicone release composition
US6124419A (en)	2000-09-26	Release modifier compositions
GB2048915A (en)	1980-12-17	Solventless release compositions methods and articles of manufacture
US5468816A (en)	1995-11-21	Silicone release compositions
EP0826732A2 (fr)	1998-03-04	Compositions de revêtement de silicone anti-adhésives
CA2088865A1 (fr)	1993-09-07	Compositions d'organosilicone
US5125998A (en)	1992-06-30	Process for improving the bath life and cure time of heat-curable silicone compositions
CN100393780C (zh)	2008-06-11	作为硅氧烷涂料组合物的防雾添加剂的支链型烯基官能硅氧烷聚合物
US5108791A (en)	1992-04-28	Heat-curable silicone compositions having improved bath life
EP0850999A2 (fr)	1998-07-01	Compositions de revêtement de silicone anti-adhésives
JPH0149745B2 (fr)	1989-10-25
US5082871A (en)	1992-01-21	UV-activation of addition cure silicon coatings
KR19980064771A (ko)	1998-10-07	실리콘 박리 피복 조성물